BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    L.P.I. LASER DELIVERY SYSTEM

    K Number: K904331 · Decision Dec 17, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    476
    Registration Numbers
    479
    Same Product Code
    2793
    Applicant Total
    14
    Review Days
    87

    Basic Information

    Device Name
    L.P.I. LASER DELIVERY SYSTEM
    K Number
    K904331
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4810
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    LASER PHOTONICS, INC.
    Date Received
    September 21, 1990
    Decision Date
    December 17, 1990
    Product Code
    GEX
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    GEX Powered Laser Surgical Instrument

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